Variants in gene ANKRD1 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_014391.3(ANKRD1):c.827C>T (p.Ala276Val)	rs35550482	0.00244
NM_014391.3(ANKRD1):c.197G>A (p.Arg66Gln)	rs150797476	0.00092
NM_014391.3(ANKRD1):c.417C>A (p.Phe139Leu)	rs201398260	0.00043
NM_014391.3(ANKRD1):c.368C>T (p.Thr123Met)	rs145387010	0.00030
NM_014391.3(ANKRD1):c.652-10A>T	rs397517252	0.00023
NM_014391.3(ANKRD1):c.346-15_346-14del	rs794728971
NM_014391.3(ANKRD1):c.346-17_346-10del	rs397517250
NM_014391.3(ANKRD1):c.346-29_346-12del	rs72003210
NM_014391.3(ANKRD1):c.346-43AT[13]	rs60406118

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